Variant report
Variant | rs2254729 |
---|---|
Chromosome Location | chr21:16448219-16448220 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
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No data |
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Variant related genes | Relation type |
---|---|
ENSG00000180530 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs1297219 | 0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1997576 | 0.93[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs2142220 | 0.93[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs2142221 | 0.93[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs2205238 | 0.92[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs2205239 | 0.93[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs2243778 | 0.85[ASW][hapmap];0.92[CEU][hapmap];0.90[MKK][hapmap];0.89[TSI][hapmap];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs2252756 | 0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2253879 | 0.93[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs2254152 | 0.94[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs2254269 | 0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs2254956 | 1.00[ASW][hapmap];0.96[CEU][hapmap];0.83[GIH][hapmap];1.00[LWK][hapmap];0.84[MEX][hapmap];0.93[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs2255190 | 1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs2403876 | 0.92[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs2776045 | 0.93[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs2823032 | 0.96[CEU][hapmap];0.84[MEX][hapmap];0.93[TSI][hapmap];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs8130770 | 0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs8132765 | 0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs8134191 | 0.92[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs972136 | 0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv834048 | chr21:16324481-16489570 | Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 19 gene(s) | inside rSNPs | diseases |
2 | nsv587050 | chr21:16413682-16462268 | Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
3 | nsv1059303 | chr21:16423727-16466112 | Enhancers Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
4 | nsv544379 | chr21:16423727-16466112 | Weak transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
5 | nsv523396 | chr21:16447754-16453356 | Enhancers Weak transcription | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr21:16440800-16450000 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |